Evidence map›Paper›PMID 25633984›Full record

ArticleJournal of biological rhythms2015

Phase resetting in duper hamsters: specificity to photic zeitgebers and circadian phase.

Emily N C Manoogian, Tanya L Leise, Eric L Bittman

Abstract read
In one paragraph

Article in Journal of biological rhythms, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Circadian Responses to Light in the BTBR Mouse.Journal of biological rhythms · 2022
    Article
  2. The duper mutation reveals previously unsuspected functions ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Emily N C ManoogianDepartment of Biology and Program in Neuroscience and Behavior, University of Massachusetts, Amherst, Massachusetts emanoogi@cns.umass.edu.
Tanya L LeiseDepartment of Mathematics & Statistics, Amherst College, Amherst, Massachusetts.
Eric L BittmanDepartment of Biology and Program in Neuroscience and Behavior, University of Massachusetts, Amherst, Massachusetts.

Funding

Suprachiasmatic Control of Peripheral Circadian RhythmsR01MH070019 · NIMH · UNIVERSITY OF MASSACHUSETTS AMHERST · PI BITTMAN, ERIC L · 2005 to 2009
$1.5M
Function and Control of Hypothalamic OscillatorsR21HD078863 · NICHD · UNIVERSITY OF MASSACHUSETTS AMHERST · PI BITTMAN, ERIC L · 2014 to 2015
$420k
NICHD NIH HHS R21 HD078863NICHD NIH HHS R21-HD078863NIMH NIH HHS R01 MH070019NIMH NIH HHS R01-MH070019,
6 · The paper itself

Abstract

The duper mutation in Syrian hamsters shortens the free-running period of locomotor activity (τDD) to about 23 h and results in a type 0 phase-response curve (PRC) to 15-min light pulses. To determine whether exaggerated phase shifts are specific to photic cues and/or restricted to subjective night, we subjected hamsters to novel wheel confinements and dark pulses during subjective day. Small phase shifts elicited by the nonphotic cue were comparable in mutant and wild-type (WT) hamsters, but dark pulses triggered larger shifts in dupers. To assess further the effects of the duper mutation on light-dark transitions, we transferred hamsters between constant light (LL) and constant dark (DD) or between DD and LL at various circadian phases. Duper hamsters displayed significantly larger phase shifts than WT hamsters when transferred from LL to DD during subjective day and from DD to LL during subjective night. The variability of phase shifts in response to all light/dark transitions was significantly greater in duper hamsters at all time points. In addition, most duper hamsters, but none of the WTs, displayed transient ultradian wheel-running patterns for 5 to 12 days when transferred from light to dark at CT 18. The χ(2) periodogram and autocorrelation analyses indicate that these ultradian patterns differ from the disruption of rhythmicity by SCN lesions or exposure to constant bright light. We conclude that the duper mutation specifically amplifies phase shifts to photic cues and may destabilize coupling of circadian organization upon photic challenge due to weakened coupling among components of the circadian pacemaker. Mathematical modeling of the circadian pacemaker supports this hypothesis.

Indexed as

Circadian RhythmMotor ActivityAnimalsBiological ClocksCricetinaeLightMesocricetusMutationPhotic StimulationSuprachiasmatic Nucleustau Proteinstau Proteinsconstant lightdark pulseduperentrainmenthamsterlight transitionsnovel wheelphase-response curvephase shiftultradian

Identifiers

PMID25633984
PMCPMC4461060

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.